CN110317551A - Adhesive tape - Google Patents
Adhesive tape Download PDFInfo
- Publication number
- CN110317551A CN110317551A CN201910247405.8A CN201910247405A CN110317551A CN 110317551 A CN110317551 A CN 110317551A CN 201910247405 A CN201910247405 A CN 201910247405A CN 110317551 A CN110317551 A CN 110317551A
- Authority
- CN
- China
- Prior art keywords
- foamed sheet
- adhesive
- adhesive tape
- resin
- methyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000002390 adhesive tape Substances 0.000 title claims abstract description 78
- 239000000853 adhesive Substances 0.000 claims abstract description 104
- 230000001070 adhesive effect Effects 0.000 claims abstract description 104
- 238000004132 cross linking Methods 0.000 claims description 18
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 17
- 229920005672 polyolefin resin Polymers 0.000 claims description 12
- 239000012790 adhesive layer Substances 0.000 claims description 3
- 229920005989 resin Polymers 0.000 description 81
- 239000011347 resin Substances 0.000 description 81
- 239000000178 monomer Substances 0.000 description 48
- 238000000034 method Methods 0.000 description 46
- -1 hydrocarbon radical Chemical class 0.000 description 34
- 150000001875 compounds Chemical class 0.000 description 29
- 239000000203 mixture Substances 0.000 description 29
- 239000004088 foaming agent Substances 0.000 description 23
- 238000012360 testing method Methods 0.000 description 22
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 18
- 229920002554 vinyl polymer Polymers 0.000 description 18
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 17
- CERQOIWHTDAKMF-UHFFFAOYSA-N alpha-methacrylic acid Natural products CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 16
- 230000008569 process Effects 0.000 description 16
- 125000005250 alkyl acrylate group Chemical group 0.000 description 15
- 238000004064 recycling Methods 0.000 description 15
- 229920001577 copolymer Polymers 0.000 description 14
- 239000003431 cross linking reagent Substances 0.000 description 14
- 238000004519 manufacturing process Methods 0.000 description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 13
- 238000005187 foaming Methods 0.000 description 13
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 12
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
- 229920001684 low density polyethylene Polymers 0.000 description 12
- 239000004702 low-density polyethylene Substances 0.000 description 12
- 150000002148 esters Chemical class 0.000 description 11
- 229920000642 polymer Polymers 0.000 description 11
- 239000006260 foam Substances 0.000 description 10
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 9
- 239000003522 acrylic cement Substances 0.000 description 9
- 229920001971 elastomer Polymers 0.000 description 9
- 239000004615 ingredient Substances 0.000 description 9
- 239000012948 isocyanate Substances 0.000 description 9
- 238000005259 measurement Methods 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 8
- 150000003505 terpenes Chemical class 0.000 description 8
- 235000007586 terpenes Nutrition 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 7
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 7
- 150000001336 alkenes Chemical class 0.000 description 7
- 239000007767 bonding agent Substances 0.000 description 7
- 239000000470 constituent Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- 239000003208 petroleum Substances 0.000 description 7
- 239000005056 polyisocyanate Substances 0.000 description 7
- 229920001228 polyisocyanate Polymers 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 229920005862 polyol Polymers 0.000 description 7
- 150000003077 polyols Chemical class 0.000 description 7
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 150000002513 isocyanates Chemical class 0.000 description 6
- 239000003446 ligand Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 229920000346 polystyrene-polyisoprene block-polystyrene Polymers 0.000 description 6
- 239000004711 α-olefin Substances 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 5
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 4
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 4
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000003426 co-catalyst Substances 0.000 description 4
- 238000005227 gel permeation chromatography Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N methylene hexane Natural products CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 4
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 4
- 239000004814 polyurethane Substances 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 150000005846 sugar alcohols Polymers 0.000 description 4
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000004902 Softening Agent Substances 0.000 description 3
- 230000006978 adaptation Effects 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 3
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 3
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000002685 polymerization catalyst Substances 0.000 description 3
- 230000002285 radioactive effect Effects 0.000 description 3
- 229910052723 transition metal Inorganic materials 0.000 description 3
- 150000003624 transition metals Chemical class 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 150000008065 acid anhydrides Chemical class 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N but-2-ene Chemical group CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 238000012790 confirmation Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
- 150000003951 lactams Chemical class 0.000 description 2
- 229920000092 linear low density polyethylene Polymers 0.000 description 2
- 239000004707 linear low-density polyethylene Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- HJYKVGWOAOLIKY-UHFFFAOYSA-N methyl 2-methylidenenonanoate Chemical compound CCCCCCCC(=C)C(=O)OC HJYKVGWOAOLIKY-UHFFFAOYSA-N 0.000 description 2
- CPOFMOWDMVWCLF-UHFFFAOYSA-N methyl(oxo)alumane Chemical compound C[Al]=O CPOFMOWDMVWCLF-UHFFFAOYSA-N 0.000 description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 230000003252 repetitive effect Effects 0.000 description 2
- 239000003566 sealing material Substances 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- 238000004078 waterproofing Methods 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- RXVMKCWWKQUKDI-UHFFFAOYSA-N (sulfonylamino)urea;toluene Chemical compound CC1=CC=CC=C1.NC(=O)NN=S(=O)=O RXVMKCWWKQUKDI-UHFFFAOYSA-N 0.000 description 1
- OTEKOJQFKOIXMU-UHFFFAOYSA-N 1,4-bis(trichloromethyl)benzene Chemical compound ClC(Cl)(Cl)C1=CC=C(C(Cl)(Cl)Cl)C=C1 OTEKOJQFKOIXMU-UHFFFAOYSA-N 0.000 description 1
- NSXOFALHYZPMNH-UHFFFAOYSA-N 1-(3-methylmorpholin-4-yl)prop-2-en-1-one Chemical compound CC1COCCN1C(=O)C=C NSXOFALHYZPMNH-UHFFFAOYSA-N 0.000 description 1
- NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 description 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical group C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 1
- HROBBUFVRGGXBM-UHFFFAOYSA-N 2,2-dimethylpropane-1,3-diol hexanedioic acid prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OCC(C)(C)CO.OC(=O)CCCCC(O)=O HROBBUFVRGGXBM-UHFFFAOYSA-N 0.000 description 1
- PUGOMSLRUSTQGV-UHFFFAOYSA-N 2,3-di(prop-2-enoyloxy)propyl prop-2-enoate Chemical compound C=CC(=O)OCC(OC(=O)C=C)COC(=O)C=C PUGOMSLRUSTQGV-UHFFFAOYSA-N 0.000 description 1
- WQNHWIYLCRZRLR-UHFFFAOYSA-N 2-(3-hydroxy-2,5-dioxooxolan-3-yl)acetic acid Chemical compound OC(=O)CC1(O)CC(=O)OC1=O WQNHWIYLCRZRLR-UHFFFAOYSA-N 0.000 description 1
- GUVXYYRRJCHAJL-UHFFFAOYSA-N 2-[8-(oxiran-2-yl)octyl]oxirane Chemical compound C1OC1CCCCCCCCC1CO1 GUVXYYRRJCHAJL-UHFFFAOYSA-N 0.000 description 1
- GTELLNMUWNJXMQ-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical class OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.CCC(CO)(CO)CO GTELLNMUWNJXMQ-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- ROGIWVXWXZRRMZ-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1 ROGIWVXWXZRRMZ-UHFFFAOYSA-N 0.000 description 1
- SKFMNMKQJBQBNA-UHFFFAOYSA-N 2-methylprop-2-enoic acid tetradecane Chemical compound C(C(=C)C)(=O)O.CCCCCCCCCCCCCC SKFMNMKQJBQBNA-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical group CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- JOLOSPPNXWGZBG-UHFFFAOYSA-N C[Ti]C1C=CC=C1 Chemical compound C[Ti]C1C=CC=C1 JOLOSPPNXWGZBG-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-N Formic acid Chemical class OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 208000037656 Respiratory Sounds Diseases 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
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- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
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- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/06—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent
- C08J9/10—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent developing nitrogen, the blowing agent being a compound containing a nitrogen-to-nitrogen bond
- C08J9/102—Azo-compounds
- C08J9/103—Azodicarbonamide
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/36—After-treatment
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F220/1804—C4-(meth)acrylate, e.g. butyl (meth)acrylate, isobutyl (meth)acrylate or tert-butyl (meth)acrylate
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/04—N2 releasing, ex azodicarbonamide or nitroso compound
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/04—Homopolymers or copolymers of ethene
- C08J2323/08—Copolymers of ethene
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/40—Additional features of adhesives in the form of films or foils characterized by the presence of essential components
- C09J2301/408—Additional features of adhesives in the form of films or foils characterized by the presence of essential components additives as essential feature of the adhesive layer
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/40—Additional features of adhesives in the form of films or foils characterized by the presence of essential components
- C09J2301/414—Additional features of adhesives in the form of films or foils characterized by the presence of essential components presence of a copolymer
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2400/00—Presence of inorganic and organic materials
- C09J2400/20—Presence of organic materials
- C09J2400/24—Presence of a foam
- C09J2400/243—Presence of a foam in the substrate
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2423/00—Presence of polyolefin
- C09J2423/04—Presence of homo or copolymers of ethene
- C09J2423/046—Presence of homo or copolymers of ethene in the substrate
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2475/00—Presence of polyurethane
Abstract
The subject of the invention is to provide the adhesive tapes that waterproofness is excellent.Solution is, adhesive tape of the invention is the adhesive tape of the adhesive phase for at least one side for having independent air bubble foamed sheet and only bubble foamed sheet being arranged in, the arithmetic average roughness Ra of at least one side of above-mentioned independent air bubble foamed sheet is 1~12 μm, the peel strength of above-mentioned adhesive phase is 1.1N/25mm or more, with a thickness of 10 μm or more.
Description
Technical field
The present invention relates to the adhesive tapes for having independent air bubble foamed sheet and adhesive phase.
Background technique
In the past, foamed sheet due to such as resiliency, thermal insulation, waterproofness and moisture resistance it is excellent, be used in article
Bale packing material will carry out the sealing material for protecting the peripheral part of component for influencing it by gas or liquid etc. to seal, incite somebody to action
The various uses such as vibration and the fender of damping of shocks, the substrate of bonding sheet.It is public in patent document 1 as specific foamed sheet
Opened so that the foamable polyolefin series resin sheet comprising thermal decomposable foaming agent is foamed and be crosslinked and the cross-linked polyolefin that obtains
Based resin foamed (referring to patent document 1).
Existing technical literature
Patent document
Patent document 1: International Publication No. 2005/007731
Summary of the invention
Problems to be solved by the invention
But in recent years, in the small communication devices such as smart phone, wearable terminal, it is desirable that high waterproof performance.Cause
This, from the viewpoint of waterproofness raising, the opening portions periphery such as gap, sim card slot for being generated between display panel and shell
Configured with liner material.Liner material needs may adapt to the flexibility of the degree of the small difference of height on adherend surface, also, needs
It is used to be temporarily fixed to the adhesiveness of allocation position.As the material for meeting such physical property, it is known that have foaming body and set
Set the adhesive tape in the adhesive phase of at least one side of the foaming body.However, requiring higher waterproof performance in recent years, it is desirable that into
The raising of the waterproofness of one step.
The present invention is proposed in view of problem above, and project is to provide the adhesive tape for showing good waterproofness.
The method used for solving the problem
The inventors of the present invention have made intensive studies, as a result, it has been found that, by for have independent air bubble foamed sheet and be arranged at this
The adhesive tape of the adhesive phase of at least one side of independent air bubble foamed sheet, and make the peel strength of adhesive phase and with a thickness of certain
More than, and make arithmetic average roughness Ra a certain range of independent air bubble foamed sheet, so that the waterproofness of adhesive tape improves,
Complete the present invention.That is, the present invention is as described below.
[1] a kind of adhesive tape has independent air bubble foamed sheet and the adhesive of at least one side of the foamed sheet is arranged in
The arithmetic average roughness Ra of layer, at least one side of above-mentioned foamed sheet is 1~12 μm, and the peel strength of above-mentioned adhesive phase is
1.1N/25mm or more, with a thickness of 10 μm or more.
[2] adhesive tape according to above-mentioned [1] is only provided with adhesive phase, above-mentioned hair in above-mentioned foamed sheet on one side
The arithmetic average roughness Ra for steeping the another side of piece is 1~12 μm.
[3] adhesive tape according to above-mentioned [1] or [2], 50% compressive strength of above-mentioned foamed sheet are 40~300kPa.
[4] adhesive tape according to any one of above-mentioned [1]~[3], the interlaminar strength of above-mentioned foamed sheet is 0.8~
3.0MPa。
[5] adhesive tape according to any one of above-mentioned [1]~[4], above-mentioned foamed sheet with a thickness of 0.1~1.5mm.
[6] adhesive tape according to any one of above-mentioned [1]~[5], the expansion ratio of above-mentioned foamed sheet is 1.2~
20cm3/g。
[7] adhesive tape according to any one of above-mentioned [1]~[6], the mean air bubble diameter of above-mentioned foamed sheet are 20
~150 μm.
[8] adhesive tape according to any one of above-mentioned [1]~[7], the degree of cross linking of above-mentioned foamed sheet are 25 mass %
More than.
[9] adhesive tape according to any one of above-mentioned [1]~[8], above-mentioned foamed sheet contain polyolefin-based resins.
[10] adhesive tape according to any one of above-mentioned [1]~[9], above-mentioned foamed sheet contain 50 matter of polyvinyl resin
Measure % or more.
[11] adhesive tape according to any one of above-mentioned [1]~[10], above-mentioned adhesive phase with a thickness of 10 μm with
It is upper and 55 μm or less.
The effect of invention
According to the present invention it is possible to provide the adhesive tape for showing good waterproofness.
Detailed description of the invention
Fig. 1 is the schematic diagram of the experimental rig for evaluating interlaminar strength in embodiment and comparative example.
Specific embodiment
Hereinafter, being explained in detail to the present invention.
[adhesive tape]
Adhesive tape of the invention is the adhesive for at least one side for having independent air bubble foamed sheet and the foamed sheet being arranged in
The adhesive tape of layer, the arithmetic average roughness Ra of at least one side of above-mentioned foamed sheet are 1.0~12 μm, the stripping of above-mentioned adhesive phase
It is 1.1N/25mm or more from intensity, with a thickness of 10 μm or more.By meeting such important document, it is good waterproofness can be obtained
Adhesive tape.
(independent air bubble foamed sheet)
< arithmetic average roughness >
Adhesive tape of the invention has the independent air bubble foamed sheet that the arithmetic average roughness Ra of at least one side is 1~12 μm
(hereinafter also referred to as foamed sheet).If the arithmetic average roughness Ra of at least one side of foamed sheet is more than 12 μm, adhesive tape
Waterproofness reduce.In addition, the arithmetic average roughness Ra in the face of foamed sheet is usually 1 μm or more.
From the viewpoint of improving the waterproofness of adhesive tape more, the arithmetic average roughness of at least one side of foamed sheet
Ra is preferably 1.0~8 μm, more preferably 1.1~4 μm, further preferably 1.2~2 μm.
In the present invention, as long as the arithmetic average roughness Ra of at least one side of foamed sheet is above range, but
It can be with the arithmetic average roughness on two sides all for above range.Wherein, it is only preferably provided with adhesive on one side in foamed sheet
Layer, the adhesive tape that the arithmetic average roughness Ra of another side is 1~12 μm.The adhesive tape is due to being only arranged adhesive in one side
Layer, therefore it is easy to manufacture, and operability when pasting to adherend is excellent.It only will be provided with bonding on one side in foamed sheet
In the case that the adhesive tape of oxidant layer is inserted between component, the face for the foamed sheet that arithmetic average roughness Ra is 1~12 μm and conduct
The component of adherend directly contacts.In this case, since the Ra of foamed sheet is small, the face of foamed sheet and the adaptation of component
Become good, waterproofness improves.Further, due to also having and inserting for only in the adhesive tape for having adhesive phase on one side
Enter to after between component, it is easily removable the advantage that.
The arithmetic average roughness Ra on the surface of foamed sheet can be straight by adjusting the degree of cross linking, the average bubble of foamed sheet
Diameter, expansion ratio etc. are adjusted.
In addition, arithmetic average roughness Ra can be measured by method documented by embodiment.
50% compressive strength > of <
50% compressive strength of foamed sheet used in the present invention is not particularly limited, preferably 40~300kPa.Have
The flexibility of the bonding sheet of foamed sheet with such 50% compressive strength is high, even if in the table for the adherend for pasting bonding sheet
Face has small difference of height, is also adapted to the difference of height, waterproofness can be improved.In addition, having with such 50%
The counter-force of the thickness direction of the bonding sheet of the foamed sheet of compressive strength is lower, and can simply be matched in narrow gap with compression state
It sets.From the viewpoint of above like that, 50% compressive strength of foamed sheet is preferably 70~250kPa, more preferably 80~
230kPa, further preferably 100~200kPa.
In addition, 50% compressive strength can be measured according to JIS K6767.
< interlaminar strength >
The interlaminar strength of foamed sheet used in the present invention is not particularly limited, preferably 0.8~3.0MPa.In this explanation
So-called interlaminar strength in book is the value for indicating the tensile strength of thickness direction.
If the interlaminar strength of foamed sheet be 3.0MPa hereinafter, if adhesive tape flexibility it is high, waterproofness becomes good.Separately
On the one hand, if the interlaminar strength of foamed sheet is 0.8MPa or more, the recycling property (rework) of adhesive tape becomes good.
Adhesive tape after being pasted on adherend, is temporarily removed sometimes in order to which position is micro-adjusted, then is pasted,
At this point, the rupture etc. of adhesive tape occurs sometimes.So-called recycling property, expression have with operability when such remove-paste again
The index of pass, the good adhesive tape of so-called recycling property refer to the few adhesive tape of the frequency ruptured when removing.
From the viewpoint of the adhesive tape of balancing good for obtaining waterproofness and recycling property, the interlaminar strength of foamed sheet is excellent
It is selected as 0.9~2.5MPa, more preferably 1.0~2.0MPa, further preferably 1.2~1.8MPa.
Interlaminar strength can be adjusted by constituting type, mean air bubble diameter of resin of foamed sheet etc..In addition, at this
Interlaminar strength can be measured by method documented by aftermentioned embodiment in specification.
< mean air bubble diameter >
The mean air bubble diameter of foamed sheet used in the present invention is not particularly limited, and preferably 20~150 μm.By for
The range of such mean air bubble diameter, so that the arithmetic average roughness Ra for being easy to foam unilateral is adjusted to above range,
The waterproofness of adhesive tape improves.
In addition, if the mean air bubble diameter of foamed sheet is 150 μm hereinafter, then applying energetically when recycling to adhesive tape
In the case where, it can prevent from being broken using around the big bubble of bubble diameter as starting point.That is, if big in foamed sheet
The bubble of bubble diameter is few, then the low density part in foamed sheet tails off, therefore inhibits the rupture generated by the part.This
Outside, consider that the mean air bubble diameter of foamed sheet is preferably 20 μm or more from viewpoints such as manufacturing costs.
From the viewpoint of waterproofness and the recycling property raising for making adhesive tape, the mean air bubble diameter of foamed sheet is preferably
140 μm hereinafter, more preferably 120 μm hereinafter, further preferably 100 μm or less.Due to the hair comprising a large amount of stingy bulb diameters
The manufacturing cost of bubble piece is got higher, therefore the lower limit value of mean air bubble diameter is preferably 30 μm or more, and more preferably 40 μm or more, into
One step is preferably 50 μm or more.
In addition, the mean air bubble diameter in the present invention is will be by the mean air bubble diameter in the direction MD that aftermentioned method measures
Average bubble diameter has been carried out with the mean air bubble diameter in the direction TD.
Mean air bubble diameter refers to the value measured by following main points.
Prepare foaming body sample of the foamed sheet as measurement for being cut into 50mm square out.It is impregnated 1 in liquid nitrogen
With razor blade along the direction MD and the difference through-thickness cutting of the direction TD after minute.Use digital microscope (Co., Ltd.
キ ー エ Application ス system " VHX-900 ") 200 times of enlarged photographs are shot to its section, to being present in each of the direction MD and the direction TD
Whole bubbles of the section of the length 2mm in direction measure bubble diameter, which is repeated 5 times.In turn, by whole bubbles
Average value is set as the mean air bubble diameter in the direction MD and the direction TD.
In addition, the direction MD refers to Machine direction (mechanical direction), it is and squeezes out the consistent directions such as direction,
And the direction TD refers to Transverse direction (transverse direction), is the direction orthogonal with the direction MD, in the hair of sheet
It is in foam (foamed sheet) and unilateral parallel direction.
< expansion ratio >
The expansion ratio of foamed sheet used in the present invention is not particularly limited, preferably 1.2~20cm3/g.By making
Expansion ratio is that may be easy to for mean air bubble diameter and 50% compressive strength being adjusted in above range in above range.This
Outside, by making expansion ratio 1.2cm3/ g or more, so that flexibility is easy to become well, waterproofness is easy to become good.Separately
On the one hand, by for 20cm3For/g hereinafter, to which mechanical strength is got higher, recycling property becomes good.
From the viewpoint of like that, expansion ratio is more preferably 3~14cm3/ g, further preferably 5~13cm3/ g, more
Further preferably 7~12cm3/g.In addition, finding out the density of foamed sheet according to JIS K7222 in the present invention, its inverse is set
For expansion ratio.
< degree of cross linking >
The degree of cross linking for the foamed sheet being used in the present invention is not particularly limited, preferably 25 mass % or more.If handed over
Connection degree is that 25 mass % or more are then easy to for mean air bubble diameter and arithmetic average roughness Ra being adjusted in above range, as
As a result, recycling property improves.By for 25 mass % or more, to be easy to for the bubble of foamed sheet miniaturizeing, furthermore each bubble
The deviation of size also tail off, recycling property and mechanical strength can be made to improve.In addition, the upper limit value of the degree of cross linking of foamed sheet is excellent
It is selected as 70 mass %.Then it is easy to improve expansion ratio if it is such upper limit value, is easy to improve flexibility.From such viewpoint
Consider, the degree of cross linking of foamed sheet is more preferably 30~65 mass %, further preferably 40~60 mass %.
The degree of cross linking can be measured by method documented by embodiment.
< independent air bubble rate >
Foamed sheet of the invention is the independent air bubble foamed sheet with independent air bubble, and independent air bubble is relative to whole bubbles
Ratio (referred to as " independent air bubble rate ") is 70% or more.Such foamed sheet is easy to ensure waterproofness.Independent air bubble rate is preferably
75% or more, more preferably 90% or more.
Independent air bubble rate can be found out according to ASTM D2856 (1998).Commercially available analyzer can enumerate dry type automatic density
Count ア キ ュ ピ ッ Network 1330 etc..
More specifically, independent air bubble rate is measured by following main points.It is square that the plane that side length is 5cm is cut out from foamed sheet
Shape and certain thickness test film.The thickness of measurement test piece calculates the apparent volume V of test film1And measurement test piece
Weight W1.Next, calculating apparent volume V shared by bubble based on following formula2.In addition, constituting the density of the resin of test film
It is set as 1g/cm3。
Apparent volume V shared by bubble2=V1-W1
Then, test film is sunk into 23 DEG C of distilled water the depth away from water surface 100mm, test film is applied through 3 minutes
Add the pressure of 15kPa.Then, test film is taken out from water and removes the moisture for being attached to test film surface, measurement test piece
Weight W2, continuous air bubbles rate F is calculated based on following formula1With independent air bubble rate F2。
Continuous air bubbles rate F1(%)={ (W2-W1)/V2}×100
Independent air bubble rate F2(%)=100-F1
< size >
The thickness of foamed sheet used in the present invention is preferably 0.1~1.5mm.It can if making with a thickness of 1.5mm or less
Enough slimmings, can be suitable for the electronic equipment of miniaturization.
From the viewpoint of like that, thickness is preferably 1mm hereinafter, more preferably 0.9mm is hereinafter, further preferably
0.8mm or less.In addition, the lower limit value of thickness is according to the relationship with mean air bubble diameter, preferably 0.1mm or more, more preferably
0.15mm or more.If the waterproofness of foamed sheet and flexibility ensure to become easy with a thickness of 0.1mm or more.
Foamed sheet is preferably the narrow foamed sheet of its width, specifically, it is preferable that be processed into thin-line-shaped foamed sheet.Such as
It can make the width 5mm or less of foamed sheet and use, it can be preferably with 3mm hereinafter, more preferably used below with 1mm.This hair
Foamed sheet waterproofness used in bright is excellent, therefore can also obtain even if in the case where such as 1mm width is made excellent
Waterproofness can be suitble to use in the electronic equipment internal of miniaturization.
The lower limit value of the width of foamed sheet is not particularly limited, and can be the width of such as 0.1mm or more, Ke Yiwei
The width of 0.2mm or more.In addition, the flat shape of foamed sheet is not particularly limited, elongate rectangular, frame-shaped, L-shaped, U is made
Shape etc. is preferably.However, other than these shapes, or other any shapes such as common quadrangle, circle.
< polyolefin-based resins >
Foamed sheet used in the present invention is preferably made of resin.The type of resin is not particularly limited, from ensuring to foam
The flexibility of the appropriateness of piece, while from the viewpoint of being easy to for mean air bubble diameter being adjusted in above range, it preferably comprises poly-
Olefin-based resin.
As polyolefin resin, polyvinyl resin, acrylic resin, vinyl-vinyl acetate copolymer etc. can be enumerated,
In preferably polyvinyl resin.
(polyvinyl resin)
As polyvinyl resin, can enumerate through Ziegler-Natta compound, Metallocenic compound, chromium oxide compounds
Polyvinyl resin obtained by equal polymerization catalysts polymerization is, it is preferable to use the polymerization catalyst polymerization by Metallocenic compound obtains
Polyvinyl resin.
In addition, as polyvinyl resin, preferably straight-chain low density polyethylene (LDPE).By using straight-chain low density polyethylene
Alkene can assign flexibility to foamed sheet, and can be realized the slimming of foamed sheet.The straight-chain low density polyethylene (LDPE) is more excellent
It is selected as the straight-chain low density polyethylene (LDPE) obtained using polymerization catalysts such as Metallocenic compounds.In addition, straight-chain low-density
Polyethylene more preferably by by ethylene (for example, relative to whole amount of monomer be 75 mass % or more, preferably 90 mass % with
On) be copolymerized with a small amount of alpha-olefin as needed and the straight-chain low density polyethylene (LDPE) that obtains.
As alpha-olefin, specifically, propylene, 1- butylene, 1- amylene, 4-methyl-1-pentene, 1- hexene, 1- can be enumerated
Heptene and 1- octene etc..Wherein, the preferably alpha-olefin of carbon atom number 4~10.
Polyvinyl resin, for example above-mentioned straight-chain low density polyethylene (LDPE) density be preferably 0.870~0.910g/cm3, more
Preferably 0.875~0.907g/cm3, further preferably 0.880~0.905g/cm3。
As polyvinyl resin, a variety of polyvinyl resins also can be used, furthermore, it is possible to be added above-mentioned density range and
Polyvinyl resin other than melting range.
(Metallocenic compound)
As Metallocenic compound, can enumerate with clipping transition metal with the unsaturated compound of pi-electron system
The compounds such as bis- (cyclopentadienyl group) metal complexes of structure.More specifically, 1 or 2 or more ring penta can be enumerated
Diene basic ring or its analog are present in the transition metal of the tetravalences such as titanium, zirconium, nickel, palladium, hafnium and platinum as ligand (ligand)
Compound.
The uniform properties of the active site of such Metallocenic compound, each active site have identical activity degree.Use metal
The polymer of cyclopentadinyl compound synthesis is since the uniformity of molecular weight, molecular weight distribution, composition, composition distribution etc. is high, will
In the case where piece crosslinking comprising the polymer for using Metallocenic compound to synthesize, it is crosslinked and uniformly carries out.As a result, can be uniform
Ground stretches, therefore even if makes foamed sheet is thin to be also easy to keep its thickness uniform.
As ligand, it can be cited for example that, cyclopentadienyl rings, indenyl rings etc..These ring type compounds can by alkyl,
Substituted hydrocarbon radical or hydrocarbon-substitution metalloid base replace.As alkyl, can enumerate for example, methyl, ethyl, various propyl, various fourths
Base, various amyls, various hexyls, 2- ethylhexyl, various heptyl, various octyls, various nonyls, various decyls, various spermaceti
Base, phenyl etc..In addition, so-called " various ", refer to comprising just, secondary, uncle, different various isomers.
In addition it is possible to use ring type compound is polymerized to substance obtained by oligomer as ligand.
Further, other than the unsaturated compound of pi-electron system, the anion of the monovalencies such as chlorine, bromine can also be used to match
Body or the anionic cheating ligand of divalent, hydrocarbon, alkoxide, aryl amide, aryl oxide, amide, aryl amide, phosphide
(phosphide), diaryl-phosphide etc..
As the transition metal comprising tetravalence, the Metallocenic compound of ligand, can enumerate for example, cyclopentadienyltitanium three
(dimethylformamide), methyl cyclopentadienyl titanium three (dimethylformamide), bis- (cyclopentadienyl group) titanium chloride, dimethyl methyl silicon
Alkyl tetramethyl-ring pentadienyl-tert-butylamides zirconium dichloride etc..
Metallocenic compound with specific co-catalyst (co-catalyst) by combining, thus in the polymerization of various alkene
Play the effect as catalyst.As specific co-catalyst, methylaluminoxane (MAO), borate compounds etc. can be enumerated.Separately
Outside, co-catalyst is preferably 10~1,000,000 moles times relative to the use ratio of Metallocenic compound, and more preferably 50~5,
000 mole times.
(acrylic resin)
In addition, can enumerate as acrylic resin for example, polypropylene, propylene-α-alkene containing 50 mass % of propylene or more
Hydrocarbon copolymer etc..They can be used alone or two or more kinds may be used.
As the alpha-olefin for constituting propylene-alpha-olefin copolymers, specifically, ethylene, 1- butylene, 1- penta can be enumerated
Alkene, 4-methyl-1-pentene, 1- hexene, 1- heptene, 1- octene etc., wherein the preferably alpha-olefin of carbon atom number 6~12.
(vinyl-vinyl acetate copolymer)
The vinyl-vinyl acetate copolymer used as polyolefin resin can be enumerated for example, excellent containing vinyl acetate
It is selected as 6~40 mass %, more preferably 12~35 mass %, the further preferably ethane-acetic acid ethyenyl of 20~33 mass %
Ester copolymer.
It in the present invention, for example, can be by different 2 such as molecular weight, the amount of the vinyl acetate of copolymer composition, fusing points
Kind or more copolymer in combination use.
In addition, vinyl-vinyl acetate copolymer used in the present invention can in addition to ethylene and vinyl acetate with
Outside, the copolymer of the vinyl alcohol also generated comprising hydrolyzing a part of vinyl acetate.
As such vinyl-vinyl acetate copolymer, can enumerate for example, Dong ソ ー Co. Ltd. system " ウ Le ト ラ セ
Application ", three well デ ュ Port Application Port リ ケ ミ カ Le Co. Ltd. systems " エ バ Off レ ッ Network ス ", Ube Industries, Ltd system " UBE
Port リ エ チ レ Application ", Asahi Chemical Industry's ケ ミ カ Le ズ Co. Ltd. system " サ Application テ ッ Network " etc..
(content of each resin)
In the case where using polyvinyl resin as polyolefin resin, the amount of polyvinyl resin is relative to composition foamed sheet
Resin total amount be preferably 50 mass % or more, more preferably 60 mass % or more, further preferably 70 mass % or more can
Substantially only to include polyvinyl resin.If the content of polyvinyl resin is 50 mass % or more, waterproofness and recycling
Property improve.
In foamed sheet comprising polyolefin resin as resin in the case where, the resin contained by foamed sheet can individually make
With polyolefin resin, but it also may include the resin other than polyolefin resin.In foamed sheet, other than comprising polyolefin resin
Resin in the case where, the ratio of the resin total amount relative to polyolefin resin is preferably 60 mass % or more, more preferably 70
Quality % or more, further preferably 80 mass % or more.
In addition, polystyrene thermoplastic elastic can be enumerated as the resin other than polyolefin resin used in foamed sheet
Various elastomers, the rubber constituents such as the ethylene, propylenes based thermoplastic elastomer such as body, EPDM etc..
(thermal decomposable foaming agent)
Foamed sheet of the invention preferably passes through will be comprising the expandable composition hair of above-mentioned resin and thermal decomposable foaming agent
Bubble is to manufacture.In addition, as thermal decomposable foaming agent, it is preferable to use thermal decomposable foaming agent of the partial size less than 18 μm.In this hair
In bright, thermal decomposable foaming agent by using partial size less than 18 μm, in addition, the degree of cross linking is adjusted to particular range, so as to
To be adjusted to the range of above-mentioned mean air bubble diameter, as a result, the recycling property of adhesive tape can be made to improve.From such viewpoint
Considering, the partial size of thermal decomposable foaming agent is preferably 2~17 μm, and more preferably 5~16 μm.
In addition, the partial size of thermal decomposable foaming agent refers to the value measured by laser diffractometry, and it is comparable to accumulate
The partial size (D50) of frequency 50%.
As thermal decomposable foaming agent, it is able to use organic foaming agent, inorganic foaming agent.As organic foaming agent, can lift
The azo-compounds, N such as azodicarboamide, azodicarboxy acid metal salt (barium azodicarboxylate etc.), azodiisobutyronitrile out,
The nitroso compounds such as N '-dinitrosopentamethylene tetramine, biruea, 4,4 '-oxygroups bis- (benzene sulfonyl hydrazides), toluene sulfonyl hydrazide
Semicarbazide compounds such as equal hydrazine derivates, toluene sulfonyl semicarbazide etc..
As inorganic foaming agent, can enumerate sour ammonium, sodium carbonate, ammonium hydrogen carbonate, sodium bicarbonate, ammonium nilrite, sodium borohydride,
Citric anhydride list sodium etc..
Wherein, from the viewpoint and economy for obtaining fine bubble, from the viewpoint of secure context, preferably azo
Close object, more preferably azodicarboamide.They can be used alone or two or more kinds may be used.
The use level of thermal decomposable foaming agent in expandable composition is relative to 100 mass parts of resin, and preferably 1~20
Mass parts, more preferably 3~18 mass parts, further preferably 5~15 mass parts.
In addition, expandable composition preferably other than above-mentioned resin and thermal decomposable foaming agent, also contains nuclei of bubbles tune
Save agent.As nuclei of bubbles regulator, the organic compound of the zinc compounds such as zinc oxide, zinc stearate, citric acid, urea can be enumerated
Deng, wherein more preferably zinc oxide.By also using nuclei of bubbles regulator other than the foaming agent of above-mentioned small particle, easily
In keeping mean air bubble diameter small, the deviation of bubble diameter can be inhibited.The use level of nuclei of bubbles regulator is relative to 100 matter of resin
Measuring part is preferably 0.1~8 mass parts, more preferably 0.2~5 mass parts, further preferably 0.3~2.5 mass parts.
Expandable composition in addition to the above ingredients, can also contain antioxidant, heat stabilizer, coloring as needed
Agent, fire retardant, antistatic agent, filling material etc. are generally used in the additive of foaming body.
(manufacturing method of independent air bubble foamed sheet)
The manufacturing method of independent air bubble foamed sheet used in adhesive tape of the invention is not particularly limited, for example, can be with
By will include that the expandable composition of resin and thermal decomposable foaming agent is crosslinked, carrying out heating sends out thermal decomposable foaming agent
Bubble, manufactures along at least one stretching in the direction TD and the direction MD.More specifically, which includes the following process (1)
~(4).
Process (1): by resin, thermal decomposable foaming agent, as needed the nuclei of bubbles regulator and other additives that cooperate
Mixing, the process for being shaped to the expandable composition (resin sheet) of sheet
Process (2): the process for being crosslinked expandable composition the expandable composition irradiation ionization property radioactive ray of sheet
Process (3): the expandable composition of crosslinking is heated, thermal decomposable foaming agent is made to foam, and obtains foamed sheet
Process
Process (4): the process for stretching foamed sheet along the direction of either or both of the direction MD or the direction TD
In process (1), the molding method of resin sheet is not particularly limited, as long as example, resin, heat decomposition type are sent out
Infusion, the nuclei of bubbles regulator cooperated as needed and other additives are supplied to extruder and carry out melting mixing, from extruder
Expandable composition is extruded as sheet and carrys out moulding resin piece.
As the method for being crosslinked expandable composition in process (2), penetrated using to resin sheet irradiation electron ray, α
The method of the ionization property radioactive ray such as line, β ray, gamma-rays.As long as the exposure of above-mentioned ionizing radiation is with resulting foamed sheet
The degree of cross linking become above-mentioned desired range mode adjust, preferably 5~15Mrad, more preferably 6~
13Mrad。
In process (3), as long as heating temperature when making thermal decomposable foaming agent foam expandable composition heating is
It is more than the blowing temperature of thermal decomposable foaming agent, but preferably 200~300 DEG C, more preferably 220~280 DEG C.
The stretching of foamed sheet in process (4) can be carried out along both directions MD and TD, can also only be carried out along one, but
It is preferred that being carried out along the two.Furthermore the stretching of foamed sheet can carry out after obtaining foamed sheet making resin sheet foam, can also be
Progress while making resin sheet foam.In addition, so that resin sheet is foamed and in the case where obtaining and stretching foamed sheet after foamed sheet,
It can not directly continue foamed sheet cooling to stretch foamed sheet in the case where maintaining molten condition when foaming, can also will foam
After piece is cooling, melting or soft state post-tensioning foamed sheet is made in foamed sheet heating again.Foamed sheet is easy to by stretching
Form thin thickness.
In process (4), foamed sheet to the stretching ratio in one of the direction MD and the direction TD or both be preferably 1.1~
5.0 times, more preferably 1.2~4.0 times, further preferably 1.5~3.3 times.Wherein, particularly preferably make the stretching times to the two
Rate is within the scope of these.By being easy to make the desired range of 50% compressive strength for such range.
In addition, if making the above-mentioned lower limit value of stretching ratio or more, then the flexibility of foamed sheet is easy to become good.It is another
Aspect if it is upper limit value hereinafter, can then foamed sheet be prevented to be broken in stretching, or be leaked out from the foamed sheet in foaming and is foamed
Gas and expansion ratio significantly reduce, and the flexibility of foamed sheet becomes well, and quality is also easy to uniformly.
In addition, as long as foamed sheet is heated to such as 100~280 DEG C, preferably 150~260 DEG C when stretching.
The foamed sheet for operating and obtaining like that above can be cut off by the known method such as punch process, be processed into and wished
The shape of prestige.
However, this manufacturing method is not limited to the above method, pass through method other than the above, it is also possible to obtain foamed sheet.
For example, can cooperate organic peroxide in advance in expandable composition by replacing irradiation ionization property radioactive ray, will foam
Property composition heating be crosslinked organic peroxide decomposition method etc..
(adhesive phase)
Adhesive tape of the invention is provided with adhesive phase in at least one side of foamed sheet.Have by the adhesive phase aftermentioned
Peel strength and thickness, so that the waterproofness of adhesive tape becomes good.
(peel strength)
The peel strength of adhesive phase is 1.1N/25mm or more.The adhesive tape pair if peel strength is less than 1.1N/25mm
The adaptation of adherend reduces, and waterproofness is deteriorated.From make adhesive tape waterproofness it is good from the viewpoint of, the removing of adhesive phase
Intensity is preferably 1.5N/25mm or more, more preferably 2N/25mm or more, further preferably 3N/25mm or more.From making to bond
From the viewpoint of the recycling property of band improves, the peel strength of adhesive phase is preferably 20N/25mm hereinafter, more preferably 15N/
25mm is hereinafter, further preferably 10N/25mm or less.The peel strength of adhesive phase can be by constituting the viscous of adhesive phase
Type of mixture etc. adjusts.
In addition, the peel strength of so-called adhesive phase, refers to according to 90 degree at 25 DEG C of JIS Z0237-2009 measurement
Peel off bonding force.
In the present invention, in the case where being provided with adhesive phase on one side, the bonding of the one side only is set in foamed sheet
Oxidant layer meets above-mentioned peel strength.In the case where the two sides of foamed sheet is provided with adhesive phase, can only one side adhesive
Layer meets above-mentioned peel strength, can also meet above-mentioned peel strength with the adhesive phase on two sides.
(thickness)
Adhesive phase used in adhesive tape of the invention with a thickness of 10 μm or more.If it is less than 10 μm, then with glued
Closely sealed between object becomes inadequate, and waterproofness is deteriorated.From the viewpoint of keeping waterproofness good, the thickness of adhesive phase is preferred
It is 15 μm or more, more preferably 18 μm or more.In addition, from the viewpoint of the electronic equipment use to miniaturization, adhesive phase
It is preferably thin to a certain degree, specifically, adhesive phase is preferably 55 μm hereinafter, more preferably 50 μm or less.If using this
The certain thickness of sample adhesive phase below, even if then in the component that adhesive tape is compressed to and is inserted into narrow electronic equipment
Between in the case where, repulsive force is also low, can prevent the deformation etc. of component.
Adhesive tape is in the case where foamed sheet two sides has adhesive phase, as long as only the adhesive phase of one side meets above-mentioned thickness
Degree, but from the viewpoint for keeping the overall thickness of adhesive tape thin, from the viewpoint of reducing repulsive force, the preferred adhesive phase on two sides
Meet above-mentioned value.
(adhesive)
Adhesive phase is preferably formed by adhesive described below.It as adhesive, is not particularly limited, for example, can be with
Using acrylic adhesive, carbamate system adhesive, elastomeric adhesive etc., from the viewpoint of recycling property and waterproofness
Consider, preferably acrylic adhesive.
In the present invention, in the case where adhesive tape has adhesive phase on foamed sheet two sides, 2 adhesive phases are used
Adhesive can be the same or different.
(acrylic adhesive)
Hereinafter, the embodiment to acrylic adhesive used in adhesive phase is described in more detail.Acrylic acid
Be adhesive be containing will comprising (methyl) alkyl acrylate system monomer (A) polymerizable monomer polymerization obtained by acrylic acid series
The adhesive of polymer.
In addition, in the present specification, so-called term " (methyl) alkyl acrylate ", refer to comprising alkyl acrylate,
With the concept of both alkyl methacrylates, other similar terms are also the same.In addition, term " polymerizable monomer ", not only
It is only the compound without repetitive unit, as long as being with the compound of (methyl) alkyl acrylate system monomer (A) copolymerization
Can, there is aftermentioned other monomers itself the compound of repetitive unit to be also included in the concept of term " polymerizable monomer ".
(methyl) alkyl acrylate system monomer (A)
(methyl) alkyl acrylate system monomer (A) is preferably the ester of (methyl) acrylic acid and aliphatic alcohol, and is rouge
The carbon atom number of the alkyl of fat race alcohol is preferably 2~14, the Arrcostab in more preferably 4~10 aliphatic alcohol source.If alkane
The carbon atom number of base is then to be easy to peel strength being adjusted to above range within the scope of this.
As specific (methyl) alkyl acrylate system monomer (A), can enumerate for example, (methyl) ethyl acrylate, (first
Base) n-propyl, (methyl) isopropyl acrylate, (methyl) n-butyl acrylate, (methyl) isobutyl acrylate, (first
Base) tert-butyl acrylate, (methyl) amyl acrylate, (methyl) Hexyl 2-propenoate, (methyl) heptylacrylate, (methyl) propylene
Sour 2- ethylhexyl, (methyl) n-octyl, (methyl) Isooctyl acrylate monomer, (methyl) nonyl acrylate, (methyl) third
Olefin(e) acid last of the ten Heavenly stems ester, (methyl) acrylic acid hendecane base ester, (methyl) dodecylacrylate, (methyl) acrylic acid tridecyl
Ester and (methyl) acrylic acid tetradecane base ester etc..
Wherein, preferably (methyl) n-butyl acrylate, (methyl) Hexyl 2-propenoate, (methyl) heptylacrylate, (first
Base) 2-EHA, (methyl) n-octyl, more preferably (methyl) n-butyl acrylate, (methyl) propylene
Sour 2- ethylhexyl or their combination.
(methyl) alkyl acrylate system monomer may be used alone, or two or more kinds may be used in combination.
Component units from (methyl) alkyl acrylate system monomer (A) constitute principal component in adhesive, contain
Amount in terms of adhesive total amount benchmark be generally 30 mass % or more, preferably 40 mass % or more, more preferably 45 weight % with
On.In this way, if keeping the content of (methyl) alkyl acrylate system monomer (A) more, it can be to desired by adhesive imparting
Bonding force.
In addition, the content of the Component units from (methyl) alkyl acrylate system monomer (A) in adhesive is with after
The content of (methyl) alkyl acrylate system monomer (A) in the adhesive composition stated is substantially the same, therefore can replace
It indicates.It is also the same about the ingredient other than (A) ingredient described below.
Vinyl monomer (B) containing polar group
Polymerizable monomer also contains preferably other than (methyl) alkyl acrylate system monomer (A) and contains polar group
Vinyl monomer (B).Vinyl monomer (B) containing polar group has polar group and vinyl.By being used in adhesive phase
Monomer (B) containing polar group, to be easy to adjust peeling bonding force of adhesive phase etc..
As the vinyl monomer (B) containing polar group, such as (methyl) acrylic acid and itaconic acid etc. can be enumerated and contain second
The carboxylic acid of alkenyl and its acid anhydride, the vinyl monomer with hydroxyl, the vinyl monomer containing nitrogen etc..
As the vinyl monomer with hydroxyl, (methyl) acrylic acid 2- hydroxy methacrylate, (methyl) acrylic acid 2- can be enumerated
Hydroxy propyl ester, (methyl) acrylic acid 4- hydroxybutyl, caprolactone modification (methyl) acrylate, polyoxyethylene (methyl) acrylic acid
Ester and polyoxypropylene (methyl) acrylate etc..
As the vinyl monomer containing nitrogen, can enumerate (methyl) acrylonitrile, n-vinyl pyrrolidone, N- vinyl oneself
Lactams, N- vinyl lauric lactam, (methyl) acryloyl morpholine, (methyl) acrylamide, dimethyl (methyl) propylene
Amide, N- methylol (methyl) acrylamide, N- butoxymethyl (methyl) acrylamide and dimethylaminomethyl (methyl)
Acrylate etc..
In vinyl monomer (B) containing polar group, preferably (methyl) acrylic acid and itaconic acid etc. contain vinyl
Carboxylic acid and its acid anhydride, more preferably (methyl) acrylic acid, further preferably acrylic acid.These contain the vinyl list of polar group
Body (B) may be used alone, or two or more kinds may be used in combination.
In the case where using vinyl monomer (B) containing polar group, is derived from adhesive and contain polar group
The content of the Component units of vinyl monomer (B) is relative to the composition list for deriving from (methyl) alkyl acrylate system monomer (A)
First 100 mass parts are preferably 1~15 mass parts, more preferably 2~12 mass parts, further preferably 3~10 mass parts.Pass through
In the range for keeping the content of the vinyl monomer (B) containing polar group such, to be easy to the Tg of adhesive phase, agglutination
Power, bonding force etc. are adjusted to range appropriate.
Other monomers
Polymerizable monomer may include other monomers other than above-mentioned (A) and (B).As other monomers, benzene can be enumerated
Vinyl esters of carboxylic acids such as vinyl monomer, polyfunctional monomer, vinyl acetate etc..As styrenic monomers, can enumerate for example,
Styrene, α-methylstyrene, o-methyl styrene and p-methylstyrene etc..
In addition, the monomer with 2 or more vinyl can be enumerated as polyfunctional monomer, can preferably enumerate with 2 with
The multifunctional (methyl) acrylate of upper (methyl) acryloyl group.If using polyfunctional monomer, acrylic acid series polymeric compounds energy
Enough form reticular structure.
As specific polyfunctional monomer, hexylene glycol two (methyl) acrylate, polyethylene glycol two (methyl) third can be enumerated
Olefin(e) acid ester, polypropylene glycol two (methyl) acrylate, Ethoxylated bisphenol A bis- (methyl) acrylate, three (2- hydroxyethyls)
Isocyanurate triacrylate, ethoxylated trimethylolpropane triacrylate, propoxylation trimethylolpropane tris third
Olefin(e) acid ester, propoxylated glyceryl triacrylate, NPGA neopentyl glycol adipate diacrylate etc..
Using other monomers, in adhesive, the content from the Component units of other monomers is opposite
In source (methyl) alkyl acrylate system monomer (A) 100 mass parts of Component units be 0.5~15 mass parts, more preferably 1
~7 mass parts, further preferably 1~5 mass parts.
The weight average molecular weight of acrylic acid series polymeric compounds measured by GPC method is not particularly limited, and for example, 200,000~100
Ten thousand, preferably 400,000~900,000.
(tackifying resin)
From the viewpoint of improving bonding force, acrylic adhesive can contain tackifying resin.As tackifying resin,
The preferably Inhibition of polymerization such as hydrogenated terpene resin, hydrogenated rosin, disproportionated rosin resin, rosin ester based polymer, Petropols
Low tackifying resin.Wherein, inhibit polymerization reaction, therefore the increasing of preferably rosin series if tackifying resin has a large amount of double bonds
Viscosity resin, wherein preferably rosin ester based polymer.
From make adhesive cohesive force and bonding force improve from the viewpoint of, as long as the softening point of tackifying resin be 95 DEG C with
Upper degree, but preferably comprising softening point is 120 DEG C or more of tackifying resin, for example, can be used together softening point be 95 DEG C with
The upper and tackifying resin less than 120 DEG C and softening point are 120 DEG C or more and 150 DEG C of tackifying resins below.In addition, softening point
As long as the ring and ball method by JISK2207 defined measures.
The content of tackifying resin in acrylic adhesive is preferably 2 relative to 100 mass parts of acrylic acid series polymeric compounds
~40 mass parts, more preferably 4~35 mass parts, further preferably 5~25 mass parts.
(crosslinking agent)
In the case where the resin for constituting acrylic adhesive has hydroxyl, carboxyl, from the viewpoint for improving adhesiveness
Consider, cross-linked structure can be formed between main chain by using crosslinking agent.
As crosslinking agent, can enumerate for example, isocyanates system crosslinking agent, epoxy crosslinking agent, aziridine system crosslinking agent and
Metal chelate crosslinking agent etc..Wherein, preferably isocyanates system crosslinking agent, epoxy crosslinking agent.
As isocyanates system crosslinking agent, can enumerate for example, polyisocyanate compound.As polyisocyanate compound
Concrete example, the fragrance such as toluene di-isocyanate(TDI), methyl diphenylene diisocyanate, benzene dimethylene diisocyanate can be enumerated
The aliphatic polyisocyantes such as race's polyisocyanates, hexamethylene diisocyanate, isophorone diisocyanate, hydrogenated diphenyl
Alicyclic polyisocyanates such as methane diisocyanate etc..In addition, can also enumerate their biuret body, isocyanuric acid ester body,
And as with the low molecules active hydrogen-contg compound such as ethylene glycol, propylene glycol, neopentyl glycol, trimethylolpropane, castor oil
Adduction body of reactant etc..
They can be used alone, two or more can also be applied in combination.
As epoxy crosslinking agent, can enumerate for example, bisphenol A type epoxy compound, bisphenol F type epoxy compound, 1,3-
Bis- (N, N- diglycidyl amino methyl) toluene, N, N, N ', N '-four glycidyl group -4,4- diaminodiphenyl-methane,
N, N, N ', N '-four glycidyl group m-xylene diamine, 1,3- bis- (N, N- diglycidyl amino methyl) hexamethylenes, 1,6-
Diglycidyl n-hexane etc..
The peel strength of adhesive phase used in the present invention can be adjusted by the amount of crosslinking agent.
From the viewpoint of the range for being readily adjusted to above-mentioned peel strength, use level from crosslinking agent to adhesive relative to
100 mass parts of acrylic acid series polymeric compounds are preferably 0.5 mass parts or more, more than more preferably 1 mass parts, also, it is preferred that being 7 matter
Part is measured hereinafter, more preferably 5 below the mass.
(other ingredients)
The acrylic adhesive being used in the present invention in addition to the above ingredients, can also contain plasticizer, softening
Agent, pigment, dyestuff, Photoepolymerizationinitiater initiater, fire retardant etc. are used in the various additives of adhesive in the past.
(elastomeric adhesive)
Elastomeric adhesive contains rubber constituent, as rubber constituent, it is preferable to use styrene-isoprene block copolymerization
Object.The diblock rate of styrene-isoprene block copolymer is preferably 25~70 mass %, more preferably 30~65 matter
Measure %, further preferably 45~60 weight %.Here so-called diblock, refer to formed by styrene and isoprene it is two embedding
Section.Styrene-isoprene block copolymer becomes 25% or more by diblock rate and shows sufficient bonding force, in addition,
By being easy to improve shear strength for 70 mass % or less.In addition, styrene-isoprene block copolymer contains in addition to two
Other than block, also there is the copolymer of the blocks such as 3 or more the three blocks formed by styrene, isoprene, styrene block.
Styrene amount in styrene-isoprene block copolymer is not particularly limited, preferably 14~24 mass %,
More preferably 15~18 mass %.If styrene amount is 14 mass % or more, becomes the high adhesive of compendency, be easy to mention
High shear strength.In addition, if being 24 mass % hereinafter, then cohesive force becomes appropriate size and is easy to show bonding force.
The molecular weight of styrene-isoprene block copolymer is not particularly limited, in terms of matter average molecular weight preferably
100,000~400,000, more preferably 150,000~250,000.In addition, so-called matter average molecular weight here, refers to and passes through GPC
The value that (gel permeation chromatography) method is measured as polystyrene conversion molecular weight.
Elastomeric adhesive preferably other than above-mentioned rubber constituent, further contains tackifying resin.Elastomeric adhesive
Various tackifying resins can be used in used tackifying resin, but it is preferable to use petroleum line resin, terpene resin, coumarone trees
Rouge.Tackifying resin can be used alone or two or more kinds may be used, but petroleum line resin is preferably used in combination and is selected from terpenes
It is at least one kind of in resin and coumarone resin.The combination of tackifying resin in this way and be easy to for peel strength being adjusted to
State range.
As petroleum line resin, can enumerate fatty family Petropols (C5 through-stone oleoresin), alicyclic ring family Petropols,
Aromatic system Petropols etc., it is preferably fatty from the viewpoint of the compatibility with styrene-isoprene block copolymer
Family Petropols.In addition, it is preferable to use the petroleum line resins that softening point is 90~120 DEG C or so for petroleum line resin.
In addition, as terpene resin, the terpene resin that softening point is 80~120 DEG C or so can be used, but from bonding force
From the viewpoint of ensuring, preferably less than 100 DEG C of terpene resin.In addition, as coumarone resin, in order to ensure cohesive force,
It the use of softening point is preferably 110~130 DEG C, more preferably 115~125 DEG C of coumarone resin.
Tackifying resin is preferably 60~250 mass parts relative to 100 mass parts of rubber constituent, more preferably 100~200 matter
Measure part, further preferably 110~180 mass parts.By making the use level of tackifying resin within the above range, so as to so that
Cohesive force is good and assigns the peeling bonding force of appropriateness.
In addition, and with petroleum line resin, at least one kind of in terpene resin and coumarone resin in the case where,
Petroleum line resin is preferably 50~200 mass parts relative to 100 mass parts of rubber constituent, preferably 60~150 mass parts, more excellent
It is selected as 60~110 mass parts.On the other hand, terpene resin is relative to 100 mass parts of rubber constituent, preferably 10~70 mass
Part, more preferably 20~60 mass parts, further preferably 30~50 mass parts.Further, coumarone resin is relative to rubber
100 mass parts of ingredient, preferably 10~60 mass parts, more preferably 15~50 mass parts, further preferably 20~40 mass
Part.
Elastomeric adhesive can contain softening agent, antioxidant, filler etc. as needed.
(carbamate system adhesive)
Carbamate system adhesive is not particularly limited, and can enumerate for example, being at least esterified polyalcohol and polyisocyanic acid
The carbamate resins etc. for closing object reaction and obtaining.As above-mentioned polyalcohol, can enumerate for example, polyether polyol, polyester it is more
First alcohol, polycarbonate polyol, polycaprolactone polyol etc..As above-mentioned polyisocyanate compound, can enumerate for example, hexichol
Dicyclohexylmethane diisocyanate, toluene di-isocyanate(TDI), hexamethylene diisocyanate etc..These carbamate system adhesives can be with
It is used alone, also two or more kinds may be used.
In addition, can be used makes polyurethane polyol and polyfunctional isocyanate system as carbamate system adhesive
The carbamate resins of curing agent reaction and acquisition.Polyurethane polyol, which can be enumerated, makes above-mentioned polyalcohol and polyisocyanates
Polyurethane polyol obtained by compound reaction or react polyalcohol and polyisocyanate compound with cahin extension agents such as diamines and
The polyurethane polyol obtained.As polyfunctional isocyanate system curing agent, as long as the chemical combination with 2 or more isocyanate group
Above-mentioned isocyanate compound can be used in object.
Carbamate system adhesive can also contain above-mentioned particle, in addition, amino other than carbamate resins
Formic acid esters system adhesive can contain tackifying resin, softening agent, antioxidant, filler etc. as needed.
(manufacturing method of adhesive phase)
It can be by that will include using acrylic adhesive about the adhesive for constituting adhesive phase
Then the heating of the adhesive composition of above-mentioned polymerizable monomer and polymerization initiator, reflux, crosslinked polymer are obtained.This
Outside, also polymerizable monomer polymerization can be made to obtain by the adhesive composition irradiation light comprising above-mentioned polymerizable monomer.
Adhesive composition may include at least one kind of of above-mentioned tackifying resin, particle and other ingredients as needed.
It is not particularly limited, can be enumerated for example, using coating in the method that at least one side of foamed sheet forms adhesive phase
The method of the coating machines coating adhesive such as machine, the method for being sprayed adhesive using sprayer, being coated with are coated with bonding using hairbrush
The method of agent, method that the adhesive phase formed on stripping film is transferred to foamed sheet etc..
The purposes > of < adhesive tape
The purposes of adhesive tape is not particularly limited, since waterproofness is excellent, preferably as such as electronic equipment internal
Sealing material use.Furthermore, it is possible to be suitble to use inside the small various mancarried electronic aids in the gap of configuration foamed sheet.As
Electronic equipment can enumerate liquid crystal display, organic el display, portable phone, camera, game station, electronic documentation, individual
Computer etc..
In the present invention, adhesive tape, which passes through, to be configured as described above between 2 components for constituting electronic equipment, it can be ensured that
Adaptation between this 2 components.
Embodiment
Illustrate the present invention in further detail by embodiment, but the present invention is not by any restriction of these examples.
[measuring method]
The measuring method of each physical property and evaluation method is as follows described.
< arithmetic average roughness Ra >
The arithmetic average roughness of foamed sheet passes through laser microscope (キ ー エ Application ス according to JIS B 0601 (2001)
Society's system, " VK-8500 ") measurement.
In addition, the measurement of arithmetic average roughness Ra to make adhesive phase formed before foamed sheet two sides carry out.
< interlaminar strength >
Fig. 1 shows the schematic diagrames of the experimental rig for evaluating interlaminar strength.It is applied in the 25mm square range of foamed sheet 11
After cloth silane coupling agent (セ メ ダ イ Application Co. Ltd. system " PPX プ ラ イ マ ー "), it is added dropwise diameter 5mm's in the center of coated portion
Bonding agent 12 (セ メ ダ イ Application Co. Ltd. system " PPX ").The aluminium that 25mm square is placed in part is added dropwise in bonding agent immediately after
Fixture 13 processed crimps foamed sheet with fixture 13.Then, foamed sheet is cut along the size of fixture 13.In the foamed sheet of cutting
Non- bonding jig 13 face be coated with silane coupling agent, coated portion center be added dropwise diameter 5mm bonding agent 12.Exist immediately after
The aluminum fixture 14 that 10mm square is placed in part is added dropwise in bonding agent, and foamed sheet is crimped with fixture 14.It will be on the periphery of fixture 14
After the bonding agent of exudation is wiped, notch 15 is introduced to foamed sheet along the size of fixture 14.It is placed 30 minutes at room temperature
Bonding agent is conserved, as interlaminar strength test sample.
Then, to testing machine (Co., Ltd. エ ー ア Application De デ イ system " テ of the load cell provided with 1kN
Application シ ロ Application universal testing machine "), interlaminar strength is installed in the unilateral mode vertical relative to draw direction of foamed sheet and is surveyed
Surely sample is used.One side of fixture was stretched vertically upward with speed 100mm/ minutes, only make the range of the 1cm square of foamed sheet into
Row splitting.The maximum loading of measurement at this time, as the 1st measurement result.Same operation is repeated 3 times, is put down
Mean value is set as interlaminar strength.
< expansion ratio >
About foamed sheet, apparent density is measured according to JIS K7222, its inverse is set as expansion ratio.
< mean air bubble diameter >
The mean air bubble diameter of foamed sheet is measured by the method that specification is recorded.
50% compressive strength > of <
About foamed sheet, 25% compressive strength is determined according to JIS K6767.
< degree of cross linking >
From the test film of foaming piece collection about 100mg, the weight A (mg) of precision weighing test film.Next, by the test
Dimethylbenzene 30cm of the piece at 120 DEG C3Middle dipping and after placing 24 hours, is taken on metal mesh with the metal mesh filter of 200 mesh
Insoluble ingredient, vacuum drying, precision weighing do not dissolve ingredient weight B (mg).By resulting value, calculated by following formula
The degree of cross linking (quality %).
The degree of cross linking (quality %)=(B/A) × 100
< independent air bubble rate >
The independent air bubble rate of foamed sheet is measured by the method that specification is recorded.
< peel strength >
The bonding force of adhesive phase is to have carried out bonding force when 90 ° of disbonded tests according to JIS Z 0237.It is specific and
Speech, bonding sheet is crimped with SUS plate, 90 degree of peeling bonding forces when measuring at 25 DEG C with speed removing in 300mm/ minutes.
< waterproofness >
Waterproofing property evaluation passes through the examination that under conditions of 23 DEG C of temperature, relative humidity 50%, will make by following methods
It tests sample and sinks to depth of water 10cm, the presence or absence of visual confirmation immersion carries out.
In addition, in this waterproofing property evaluation, after making test specimen, under conditions of 23 DEG C of temperature, relative humidity 50%
Maintenance carries out after 6 hours.
Evaluation criteria is will to be set as the case where the inside of frame shape is not soaked after 1 hour after sinking to depth of water 10cm
30 minutes are not had the case where soaking, soaking within 1 hour to set the case where being set as " A ", will soak within 30 minutes by " S "
It is evaluated for " B ".
(production of test specimen)
It is vertical 60mm × horizontal 40mm, the frame shape that width is 1.0mm that adhesive tape, which is punched into periphery,.It then, will be resulting
The adhesive tape of frame-shaped with arithmetic average roughness Ra is 1.0 μm, 2 blocks of acrylic acid tie-plates that maximum height roughness Rz is 5.0 μm
It clips.In turn, with bolt fastening until the gap between 2 blocks of acrylic acid tie-plates becomes half.
Then, which is sunk into depth of water 10cm by the above method, visual confirmation is in the inside water of frame-shaped
No immersion.
< recycling property evaluation test >
Adhesive tape is cut into length 30cm, width 25mm, in such a way that air does not enter, on SUS plate, makes adhesive tape
Adhesive phase contact, on adhesive tape load 2kg roller and it is reciprocal 2 back and forth, adhesive phase is crimped with SUS plate.Then,
Disbonded test is carried out with 300mm/min using cupping machine (テ Application シ ロ Application), is shelled at the interface of adhesive phase and SUS plate
From " A: flawless " being evaluated as if not remaining foaming body on SUS plate after removing, if after removing on SUS plate
Residual foaming body is then evaluated as " B: crackle ".
[resin]
Resin used in the present embodiment described below.
Resin A (LLDPE): straight-chain ldpe resin (LLDPE) (エ Network ソ Application ケ ミ カ Le society system, quotient
The name of an article " EXACT3027 ", density: 0.900)
[manufacture of adhesive phase]
The manufacture > of < adhesive phase A
70 mass parts of butyl acrylate, acrylic acid 2- second are put into the reactor for having thermometer, blender, cooling tube
Own 25 mass parts of ester of base and 5 mass parts of acrylic acid are further added 80 mass parts of ethyl acetate, have carried out nitrogen displacement.Then,
Reactor is heated and starts to flow back.Then, in above-mentioned reactor, the azodiisobutyronitrile as polymerization initiator is added
0.1 mass parts flow back 5 hours at 70 DEG C, obtain the solution of acrylic acid series copolymer.
About resulting acrylic acid series copolymer, uses Water society system " 2690SeparationsModel " as column, lead to
It crosses GPC method and determines weight average molecular weight, result is 500,000.
In the solution of resulting acrylic acid series copolymer (100 mass parts) cooperate 1 mass parts of isocyanates system crosslinking agent,
10 mass parts of polymer of rosin ester system, are stirred, to obtain adhesive.The adhesive is coated on as described later de-
On mould paper, make it dry to obtain adhesive phase A.
The manufacture > of < adhesive phase B
Butyl acrylate is changed to 55 mass parts, 2-EHA is changed to 40 mass parts, by isocyanic acid
Ester system crosslinking material is changed to 3 mass parts, and the polymer of rosin ester system is changed 5 parts, in addition to this, by with above-mentioned adhesive phase
The same method of A obtains adhesive.The adhesive is coated on as described later on processing release paper and is made it dry, to obtain viscous
Mixture layer B.
The composition etc. of each adhesive phase is shown in Table 1.
Table 1
[embodiment 1]
(manufacture of foamed sheet)
8 mass of azodicarboamide for being 15 μm by 100 mass parts of Resin A, as the partial size of thermal decomposable foaming agent
Part, as zinc oxide (Sakai Chemical Industry Co., Ltd.'s system, trade name " OW-212F ") 1 mass parts of nuclei of bubbles regulator and anti-
0.5 mass parts of oxidant are supplied to extruder, the melting mixing at 130 DEG C, and resulting expandable composition is squeezed out strip
The resin sheet of shape.
Next, will set the electron ray 9Mrad of the two sides irradiation acceleration voltage 500kV of the resin sheet of above-mentioned strip
After the crosslinking of rouge piece, the resin sheet of crosslinking is continuously fed to be maintained at 250 DEG C of foaming by hot wind and infrared heater
Heating is carried out in furnace makes its foaming, obtains foamed sheet.
Then, resulting foamed sheet is continuously sent out from foaming furnace.In turn, foamed sheet is maintained with the temperature on its two sides
In the state of 200~250 DEG C, stretch foamed sheet with 2.5 times of stretching ratio along its direction TD, and with foamed sheet to hair
The feeding speed (feed speed) of bubble furnace winds foamed sheet compared to fast winding speed to draw foamed sheet also along the direction MD
Reach 2.0 times.The foamed sheet (thickness: 500 μm) of embodiment 1 is obtained as a result,.In addition, the winding speed of above-mentioned foamed sheet is examined
It is adjusted caused by the foaming for considering resin sheet itself to the swell increment in the direction MD.By resulting foamed sheet according to above-mentioned evaluation side
Method evaluation, the results are shown in table 1.
(manufacture of adhesive tape)
The processing release paper for preparing 150 μm of thickness, the adhesive to form adhesive phase is coated in the demoulding process face of the processing release paper
(A), 5 minutes dry at 100 DEG C, to form 20 μm of thickness of adhesive phase, it is bonded with the one side of foamed sheet.Obtain use
The processing release paper that 150 μm of thickness covers the adhesive tape of single side.
[embodiment 2~9 and comparative example 1~3]
The composition of expandable composition, electronbeam irradiation condition, the type of adhesive phase, thickness etc. is as shown in table 2
It changes like that, in addition to this, operates similarly with example 1 and obtain foamed sheet and adhesive tape.The stretching ratio of MD and TD
It is adjusted in the range of 1.5~3.0.Resulting foamed sheet is evaluated according to above-mentioned evaluation method, the results are shown in table 2
In.
By embodiment it is found that the waterproofness of adhesive tape of the invention is good.It is further known that making to foam in embodiment
In the case that the interlaminar strength of piece is a certain range, recycling property becomes good.In contrast, it is unsatisfactory for important document of the invention
Adhesive tape shown in comparative example becomes the result of waterproofness difference.
The explanation of symbol
11 foamed sheets
12 bonding agents
13,14 fixture
15 notch.
Claims (11)
1. a kind of adhesive tape has independent air bubble foamed sheet and the adhesive phase at least one face of the foamed sheet is arranged in,
The arithmetic average roughness Ra of at least one side of the foamed sheet is 1~12 μm,
The peel strength of described adhesive layer is 1.1N/25mm or more, with a thickness of 10 μm or more.
2. adhesive tape according to claim 1 is only provided with adhesive phase, the foamed sheet in the foamed sheet on one side
Another side arithmetic average roughness Ra be 1~12 μm.
3. adhesive tape according to claim 1 or 2,50% compressive strength of the foamed sheet is 40~300kPa.
4. adhesive tape described in any one of claim 1 to 3, the interlaminar strength of the foamed sheet is 0.8~3.0MPa.
5. adhesive tape according to any one of claims 1 to 4, the foamed sheet with a thickness of 0.1~1.5mm.
6. adhesive tape according to any one of claims 1 to 5, the expansion ratio of the foamed sheet is 1.2~20cm3/g。
7. adhesive tape described according to claim 1~any one of 6, the mean air bubble diameter of the foamed sheet is 20~150 μ
m。
8. adhesive tape according to any one of claims 1 to 7, the degree of cross linking of the foamed sheet is 25 mass % or more.
9. adhesive tape described according to claim 1~any one of 8, the foamed sheet contains polyolefin-based resins.
10. adhesive tape described according to claim 1~any one of 9, the foamed sheet contains 50 mass % of polyvinyl resin
More than.
11. adhesive tape described according to claim 1~any one of 10, described adhesive layer with a thickness of 10 μm or more and 55
μm or less.
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JP2018-069802 | 2018-03-30 | ||
JP2018069802A JP7020984B2 (en) | 2018-03-30 | 2018-03-30 | Adhesive tape |
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CN110317551A true CN110317551A (en) | 2019-10-11 |
CN110317551B CN110317551B (en) | 2023-12-01 |
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CN (1) | CN110317551B (en) |
Cited By (1)
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WO2023040386A1 (en) * | 2021-09-15 | 2023-03-23 | 苏州德佑新材料科技股份有限公司 | Rework adhesive tape and peeling method therefor |
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JP2022062494A (en) * | 2020-10-08 | 2022-04-20 | 木原産業株式会社 | Sticking material for repairing the inner sides of shoes |
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JP2004323842A (en) * | 2003-04-11 | 2004-11-18 | Sekisui Chem Co Ltd | Crosslinked polyolefin resin foamed sheet and pressure-sensitive adhesive tape |
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JP2012072393A (en) * | 2010-08-31 | 2012-04-12 | Sekisui Plastics Co Ltd | Foamed pressure-sensitive adhesive sheet |
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JP7020984B2 (en) | 2022-02-16 |
JP2019178293A (en) | 2019-10-17 |
CN110317551B (en) | 2023-12-01 |
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